Literature DB >> 20260947

Bilateral familial phaeochromocytomata with paroxysmal hypertension; successful surgical removal of tumors in two cases, with discussion of certain diagnostic procedures and physiological considerations.

E CALKINS, J E HOWARD.   

Abstract

Entities:  

Keywords:  TUMORS/pheochromocytoma

Mesh:

Year:  1947        PMID: 20260947     DOI: 10.1210/jcem-7-7-475

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


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  1 in total

1.  [The pheochromocytoma as a dominant hereditary dysgenetic tumor].

Authors:  C von DOEPP
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1962
  1 in total

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